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Comparison of efficacy and outcome of airway device-Proseal Laryngeal mask airway with Endotracheal tube under low flow anesthesia.

Comparative evaluation of efficacy and outcome of Proseal laryngeal mask airway versus cuffed endotracheal tube under Low Flow Anesthesia.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/05/014325
Enrollment
60
Registered
2018-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Adult ASAPS-I and II patients

Interventions

None listed

Sponsors

Medical college and SSGHospital Baroda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Weight- 40 to 70 kg 2. ASA PS- I and II 3. Patients Undergoing planned surgeries under GA of Duration of 45-120 minutes.

Exclusion criteria

Exclusion criteria: 1.Patients with likely difficult airway 2.Patients with Gastro esophageal reflux disease 3.Patients with full stomach 4.Patients with known allergy to latex 5.Recent history of sore throat or common cold with in last 10 days 6.Patients with acute or chronic cardiovascular diseases, respiratory diseases, renal or liver insufficiency. 7.Patients who consume alcohol and who smoke 8.Patient not willing to participate in the study.

Design outcomes

Primary

MeasureTime frame
1) To compare safety and efficacy of P-LMA versus ETT using ventilatory parameters to assess feasibility of airway device during low flow anaesthesia The parameter comprises of Oropharyngeal leak pressureTimepoint: 1) To compare safety and efficacy of P-LMA versus ETT using ventilatory parameters to assess feasibility of airway device during low flow anaesthesia The parameter comprises of Oropharyngeal leak pressure 5 min after insertion of airway device.

Secondary

MeasureTime frame
1.Inspired and Expired tidal volume and their difference 2. Peak / plateau pressure 3. To assess respiratory parameters during low flow anaesthesia a)Inspired and Expired Isoflurane concentration b)Continuous monitoring of ETCO2(iCO2) c)Inspired and expired N2O concentration d)Fraction of inspired oxygen(FiO2) 4.To observe for hemodynamic changes and post-operative complications of both devices if any Timepoint: 1,5,10,20,30,40,50,60,90,120 min

Countries

India

Contacts

Public ContactDr Tamanna Solanki

Dept. of Anesthesiology, Medical College, Baroda

mgpatel111@yahoo.com9825453024

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026